Seasonal and ontogenetic variation of skin microbial communities and relationships to natural disease dynamics in declining amphibians. Issue 7 (July 2015)

• Record Type: Journal Article
• Authors: Longo, Ana V.; Savage, Anna E.; Hewson, Ian; Zamudio, Kelly R.
• Is Part Of: Royal Society open science. Volume 2:Issue 7(2015)
• Publication Date: 2015-07
• Subjects: community fingerprinting -- 16S amplicon sequencing -- dysbiosis -- Eleutherodactylus coqui -- Lithobates yavapaiensis -- host–pathogen dynamics; Science -- Periodicals; 500
• DOI: 10.1098/rsos.140377
• Languages: English
• ISSNs: 2054-5703

Abstract

Abstract : Recently, microbiologists have focused on characterizing the probiotic role of skin bacteria for amphibians threatened by the fungal disease chytridiomycosis. However, the specific characteristics of microbial diversity required to maintain health or trigger disease are still not well understood in natural populations. We hypothesized that seasonal and developmental transitions affecting susceptibility to chytridiomycosis could also alter the stability of microbial assemblages. To test our hypothesis, we examined patterns of skin bacterial diversity in two species of declining amphibians ( Lithobates yavapaiensis and Eleutherodactylus coqui ) affected by the pathogenic fungus Batrachochytrium dendrobatidis ( Bd ). We focused on two important transitions that affect Bd susceptibility: ontogenetic (from juvenile to adult) shifts in E. coqui and seasonal (from summer to winter) shifts in L. yavapaiensis . We used a combination of community-fingerprinting analyses and 16S rRNA amplicon sequencing to quantify changes in bacterial diversity and assemblage composition between seasons and developmental stages, and to investigate the relationship between bacterial diversity and pathogen load. We found that winter-sampled frogs and juveniles, two states associated with increased Bd susceptibility, exhibited higher diversity compared with summer-sampled frogs and adult individuals. Our findings also revealed that hosts harbouring higher bacterial diversity carried lower Bd infections, providing support for the protective role of bacterial communities. Ongoing work to understand skin microbiome resilience after pathogen disturbance has the potential to identify key taxa involved in disease resistance.